Naloxone Hydrochloride

Product NDC

55154-6998

11-digit product format

551546998

Labeler code

55154

Product ID

55154-6998_32035f68-f01e-44b4-ac8c-0d2daa7cf222

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

NALOXONE HYDROCHLORIDE

Dosage form

INJECTION, SOLUTION

Route

INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS

Labeler

Cardinal Health

Application

ANDA070172

Marketing category

ANDA

Marketing start

2012-03-06

Marketing end

2019-03-31

Substance

NALOXONE HYDROC

Active strength

0 mg/mL

Pharmacologic classes

Opioid Antagoni

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record